[Central neurocytoma. Immunohistochemical study: MIB1, p53 and bcl-2. Report of 5 cases].

E Uro-Coste, P Bousquet, P Arrue, M B Delisle
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Abstract

To further characterize central neurocytoma, a rare intraventricular tumour described in 1982, we analyzed six tumours by immunohistochemistry for MIB1, p53 and bcl-2. bcl-2, an inhibitor of p53-mediated apoptosis is frequently expressed in gliomas, especially in tumors with wild-type p53. Its expression in peripheral neuroblastomas suggests a down-regulation during final terminal differentiation. Six tumors from five patients (one female/four males, age ranged from 18 to 63 years) were examined. All patients were alive from 2 to 88 months after initial surgical resection. On histological sections, tumours demonstrated a typical pattern. Synaptophysin staining was seen in all cases. Proliferation index was low (< 4.5%). bcl-2 was never expressed. p53 expression varied but within low values (< 10% of cells). These latter antibodies were rarely analyzed until now in this usually benign neoplasm which represents a well differentiated variant of neuron derived tumors.

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(中央neurocytoma。免疫组化检测:MIB1、p53、bcl-2。报告5例]。
中枢神经细胞瘤是1982年发现的一种罕见的脑室内肿瘤,为了进一步表征它的特征,我们用免疫组化方法分析了6个肿瘤中MIB1、p53和bcl-2的表达。Bcl-2是一种p53介导的细胞凋亡抑制剂,常在胶质瘤中表达,尤其是在p53野生型的肿瘤中。它在周围神经母细胞瘤中的表达在末梢分化过程中下调。我们检查了5例患者的6个肿瘤(1女4男,年龄从18岁到63岁)。所有患者在手术切除后2 - 88个月存活。在组织学切片上,肿瘤表现出典型的模式。所有病例均见突触体素染色。增殖指数低(< 4.5%)。Bcl-2未表达。P53表达变化,但在低值(< 10%的细胞)。这些后一种抗体直到现在才在这种通常是良性的肿瘤中被分析,它代表了神经元源性肿瘤的一种分化良好的变体。
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